UNIVERSAL VENTED & NON/VOLUME INFUS-

UNIVERSAL VENTED & NON/VOLUME INFUS- is an FDA 510(k)-cleared medical device (K833034) manufactured by Y. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 1983. Regulation: 8.